Ohshima Toshio, Hirasawa Motoyuki, Tabata Hidenori, Mutoh Tetsuji, Adachi Tomoko, Suzuki Hiromi, Saruta Keiko, Iwasato Takuji, Itohara Shigeyoshi, Hashimoto Mistuhiro, Nakajima Kazunori, Ogawa Masaharu, Kulkarni Ashok B, Mikoshiba Katsuhiko
Laboratory for Developmental Neurobiology, RIKEN Brain Science Institute, Wako, Saitama 351-0198, Japan.
Development. 2007 Jun;134(12):2273-82. doi: 10.1242/dev.02854. Epub 2007 May 16.
The mammalian cerebral cortex consists of six layers that are generated via coordinated neuronal migration during the embryonic period. Recent studies identified specific phases of radial migration of cortical neurons. After the final division, neurons transform from a multipolar to a bipolar shape within the subventricular zone-intermediate zone (SVZ-IZ) and then migrate along radial glial fibres. Mice lacking Cdk5 exhibit abnormal corticogenesis owing to neuronal migration defects. When we introduced GFP into migrating neurons at E14.5 by in utero electroporation, we observed migrating neurons in wild-type but not in Cdk5(-/-) embryos after 3-4 days. Introduction of the dominant-negative form of Cdk5 into the wild-type migrating neurons confirmed specific impairment of the multipolar-to-bipolar transition within the SVZ-IZ in a cell-autonomous manner. Cortex-specific Cdk5 conditional knockout mice showed inverted layering of the cerebral cortex and the layer V and callosal neurons, but not layer VI neurons, had severely impaired dendritic morphology. The amount of the dendritic protein Map2 was decreased in the cerebral cortex of Cdk5-deficient mice, and the axonal trajectory of cortical neurons within the cortex was also abnormal. These results indicate that Cdk5 is required for proper multipolar-to-bipolar transition, and a deficiency of Cdk5 results in abnormal morphology of pyramidal neurons. In addition, proper radial neuronal migration generates an inside-out pattern of cerebral cortex formation and normal axonal trajectories of cortical pyramidal neurons.
哺乳动物的大脑皮层由六层组成,这些层是在胚胎期通过协调的神经元迁移产生的。最近的研究确定了皮层神经元径向迁移的特定阶段。在最后一次分裂后,神经元在脑室下区-中间区(SVZ-IZ)内从多极形态转变为双极形态,然后沿着放射状胶质纤维迁移。缺乏Cdk5的小鼠由于神经元迁移缺陷而表现出异常的皮质发生。当我们在胚胎第14.5天通过子宫内电穿孔将绿色荧光蛋白(GFP)导入迁移的神经元时,3-4天后我们在野生型胚胎中观察到了迁移的神经元,而在Cdk5基因敲除(-/-)胚胎中则未观察到。将Cdk5的显性负性形式导入野生型迁移神经元中,以细胞自主方式证实了SVZ-IZ内多极到双极转变的特异性损伤。皮层特异性Cdk5条件性敲除小鼠表现出大脑皮层分层倒置,第V层和胼胝体神经元,但第VI层神经元的树突形态严重受损。Cdk5缺陷小鼠大脑皮层中树突蛋白Map2的含量减少,皮层内皮层神经元的轴突轨迹也异常。这些结果表明,Cdk5是多极到双极正常转变所必需的,Cdk5的缺乏会导致锥体神经元形态异常。此外,适当的径向神经元迁移会产生大脑皮层由内向外的形成模式以及皮层锥体神经元正常的轴突轨迹。